C E Beerens

Author PubWeight™ 10.78^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases.	Nat Genet	1999	1.76
2	DNA-binding and strand-annealing activities of human Mre11: implications for its roles in DNA double-strand break repair pathways.	Nucleic Acids Res	2001	1.38
3	Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporter.	J Biol Chem	1998	1.02
4	Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharides.	J Clin Invest	1991	0.97
5	Glucose transport in lysosomal membrane vesicles. Kinetic demonstration of a carrier for neutral hexoses.	J Biol Chem	1990	0.93
6	Functional reconstitution of the lysosomal sialic acid carrier into proteoliposomes.	Proc Natl Acad Sci U S A	1992	0.82
7	Sialic acid storage disorders: observations on clinical and biochemical variation.	Dev Neurosci	1991	0.81
8	Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage disease.	FEBS Lett	1999	0.81
9	Nucleotide-activated chloride channels in lysosomal membranes.	Biochem Biophys Res Commun	1992	0.81
10	Characterization of a heavy metal ion transporter in the lysosomal membrane.	FEBS Lett	1998	0.77
11	Fibroblast silver loading for the diagnosis of Menkes disease.	J Med Genet	1998	0.76